Mucinex Instasoothe Lozenge
Product Images NDC 72854-267

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mucinex Instasoothe (NDC 72854-267). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Reckitt Benckiser Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Label (72854 267 Label 1)

Label (72854 267 Label 1)
Mucinex InstaSoothe Cough medicated drops label featuring Dextromethorphan HBr 5 mg as the active ingredient. The label highlights a 3-in-1 formula for cough relief lasting up to 4 hours. The drops are sugar-free and mixed berry flavor. Package contains 20 oral lozenges. Labeler is Reckitt Benckiser LLC.*
FDA Label Image

Label (72854 267 Label)

Label (72854 267 Label)
Drug Facts panel for MUCINEX INSTASOOTHE COUGH lozenges containing 5 mg Dextromethorphan Hydrobromide. Includes active ingredient purpose, uses for temporary relief of coughing, warnings, directions for adults and children, storage instructions, inactive ingredients, and company contact information. Also features a barcode and an image of a red lozenge.*
FDA Label Image

Label (Screenshot 2024 01 02 160917)

Label (Screenshot 2024 01 02 160917)
Dosage instructions table for Mucinex Instasoothe Cough lozenges containing Dextromethorphan Hydrobromide. It details dosage for adults and children 12 years and older, children 6 to under 12 years, and advises not to use in children under 6 years. Instructions include how many lozenges to take and frequency limits within 24 hours.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.